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Hu X, Tao M, Ma Z, Zhang Y, Li Y, Liang D. Regioselective Photocatalytic Dialkylation/Cyclization Sequence of 3‐Aza‐1,5‐dienes: Access to 3,4‐Dialkylated 4‐Pyrrolin‐2‐ones. Adv Synth Catal. [DOI: 10.1002/adsc.202200183] [Reference Citation Analysis]
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Liu Y, Zhang T, Wan JP. Ultrasound-Promoted Synthesis of α-Thiocyanoketones via Enaminone C═C Bond Cleavage and Tunable One-Pot Access to 4-Aryl-2-aminothiazoles. J Org Chem 2022. [PMID: 35616657 DOI: 10.1021/acs.joc.2c00708] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
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Xu Z, Geng X, Cai Y, Wang L. A Straightforward Approach to Fluorinated Pyrimido[1,2-b]indazole Derivatives via Metal/Additive-Free Annulation with Enaminones, 3-Aminoindazoles, and Selectfluor. J Org Chem 2022. [PMID: 35486919 DOI: 10.1021/acs.joc.2c00136] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 3.0] [Reference Citation Analysis]
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Ge D, Sun LW, Yu ZL, Luo XL, Xu P, Shen ZL. Regioselective synthesis of 6-nitroindole derivatives from enaminones and nitroaromatic compounds via transition metal-free C-C and C-N bond formation. Org Biomol Chem 2022. [PMID: 35107115 DOI: 10.1039/d1ob02443d] [Reference Citation Analysis]
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Guo Y, Liu Y, Wan J. Amine-catalyzed synthesis of N2-sulfonyl 1,2,3-triazole in water and the tunable N2-H 1,2,3-triazole synthesis in DMSO via metal-free enamine annulation. Chinese Chemical Letters 2022;33:855-8. [DOI: 10.1016/j.cclet.2021.08.003] [Cited by in Crossref: 7] [Cited by in F6Publishing: 8] [Article Influence: 7.0] [Reference Citation Analysis]
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Dong L, Zhang S, Zhang W, Dong Y, Mo L, Zhang Z. Synthesis, characterization and application of magnetic biochar sulfonic acid as a highly efficient recyclable catalyst for preparation of spiro-pyrazolo[3,4-b]pyridines. Res Chem Intermed. [DOI: 10.1007/s11164-022-04660-6] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 1.0] [Reference Citation Analysis]
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Liu D, Lu X, Zhang Q, Zhao Y, Zhang B, Sun Y, Dai W, Xu Y, Yu F. Facile approach to multifunctionalized 5-alkylidene-3-pyrrolin-2-ones via regioselective oxidative cyclization of 2,4-pentanediones with primary amines and sodium sulfinates. Org Chem Front . [DOI: 10.1039/d2qo00473a] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
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He J, Yang Z, Zhou X, Li Y, Gao S, Shi L, Liang D. Exploring the regioselectivity of the cyanoalkylation of 3-aza-1,5-dienes: photoinduced synthesis of 3-cyanoalkyl-4-pyrrolin-2-ones. Org Chem Front . [DOI: 10.1039/d2qo00918h] [Reference Citation Analysis]
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Guo H, Liu Y, Wen C, Wan J. Electrochemical enaminone C–H thiolation/C–N amination cascade for thiazole synthesis and its diastereoselective dearomatization. Green Chem . [DOI: 10.1039/d2gc01644c] [Cited by in Crossref: 3] [Cited by in F6Publishing: 4] [Article Influence: 3.0] [Reference Citation Analysis]
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Wen S, Tian Q, Chen Y, Zhang Y, Cheng G. Annulation of CF3-Imidoyl Sulfoxonium Ylides with 1,3-Dicarbonyl Compounds: Access to 1,2,3-Trisubstituted 5-Trifluoromethylpyrroles. Org Lett 2021;23:7407-11. [PMID: 34543038 DOI: 10.1021/acs.orglett.1c02598] [Cited by in Crossref: 6] [Cited by in F6Publishing: 10] [Article Influence: 3.0] [Reference Citation Analysis]
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Liu T, Wan JP, Liu Y. Metal-free enaminone C-N bond cyanation for the stereoselective synthesis of (E)- and (Z)-β-cyano enones. Chem Commun (Camb) 2021;57:9112-5. [PMID: 34498638 DOI: 10.1039/d1cc03292e] [Cited by in Crossref: 16] [Cited by in F6Publishing: 17] [Article Influence: 8.0] [Reference Citation Analysis]
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Lin Y, Jin J, Wang C, Wan JP, Liu Y. Electrochemical C-H Halogenations of Enaminones and Electron-Rich Arenes with Sodium Halide (NaX) as Halogen Source for the Synthesis of 3-Halochromones and Haloarenes. J Org Chem 2021;86:12378-85. [PMID: 34392684 DOI: 10.1021/acs.joc.1c01347] [Cited by in Crossref: 14] [Cited by in F6Publishing: 16] [Article Influence: 7.0] [Reference Citation Analysis]
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Duan X, Li H, Li W, Wang J, Liu N. NBS‐Promoted C−H Amination of Enaminones for the Synthesis of N‐Heterocycle Substituted Enaminones**. ChemistrySelect 2021;6:6478-82. [DOI: 10.1002/slct.202101726] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]
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